FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

METALASER VASCULASE

K Number: K883541 · Decision Nov 4, 1988
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
13
Review Days
77

Basic Information

Device Name
METALASER VASCULASE
K Number
K883541
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
METATECH CORP.
Date Received
August 19, 1988
Decision Date
November 4, 1988
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

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Other Clearances by METATECH CORP.

K Number Device Name
K924314 MOBILE STANDING FRAME
K915370 COPPER VAPOR LASER SYSTEM
K903883 VASCULASE(R) COPPER VAPOR LASER SYST, PIGMENT LES
K890865 HEXASCAN SCANNER HANDPIECE
K883881 MODIFIED MODEL 2001 FIBER OPTICS CATHETER
K883518 EVENT MARKER & A SECOND PRESSURE TREND OUTPUT
K882552 METATECH ROBINSON BOLT ACCESSORY
K882367 METATECH MICROCLIP APPLICATOR
K882286 EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET
K881447 METATECH METAL MICROCLIP
Search all 13 clearances from METATECH CORP. →